Pressurized Injectable Mouthpiece

ABSTRACT

An pressurized injectable mouthpiece for athletes in contact sports and other activities. The present invention is configured to be used at an pressurized fashion and is able to be injected with an gel-like supplement. The pressurized injectable mouthpiece comprises of an tab at the front base of the mouthpiece. Further, the present invention comprises suction vents throughout the outer base portion of the mouthpiece. The pressurized injectable mouthpiece further comprises air pockets coupled throughout the inner portion of the mouthpiece allowing the present invention to be used at an pressurized fashion.

BACKGROUND OF THE INVENTION Field of the Invention

The present invention relates to an mouthpiece for athletes in physicalcontact sports etc. More specifically, the invention relates to anmouthpiece that is configured to be pressurized in conjunction with theamount of pressure applied upon the unit and further configured to beinjected with an gel-like supplement.

BRIEF SUMMARY OF THE PRESENT INVENTION

The present invention relates to an pressurized injectable mouthpiece.The invention is configured to be injected with an supplement preferredby an individual. Further, the present invention comprises an tab at thefront base of the mouthpiece and lip guard for enclosing the injectinghole. In addition, the present invention comprises suction ventsengraved at the top outer base of the mouthpiece allowing an supplementto escape from an specific portion of the mouthpiece. Additionally, thepresent invention includes an extended region comprising an plurality ofchannels which allow supplement to be disturbed throughout thepressurized chamber at different regions. The invention comprises anplurality of air pockets that allow the entire mouthpiece to be used ina regulated pressurized fashion when bitten upon. The overallstructuring of the pressurized injectable mouthpiece can be an rubberlike material such as ethyl vinyl acetate (EVA), Kraton styrene polymermaterial, PVC, ENGAGE, or polyethylene polymer that's further formed byan molding or 3D-printed process method.

Referring to the present invention extended region for use of reference,in prior art(s) U.S. patent application Ser. No. 15/365,067 teaches anextension segment that extends from the mouthpiece, further the exteriorsegment is coupled to a distal end of the extension segment relative tothe mouthpiece. Furthermore, the exterior segment extends outwardlyaround the extension segment and opposite ends of the exterior segmentare curved back towards said mouthpiece extending away from theextension segment. The present invention extended region overcomes theprior art(s) by providing an extended region that comprises an pluralityof channels which can distribute an supplement at different regions ofthe mouthpiece. In conclusion, the present invention comprisesintroducing a new type and use of sports mouthpiece for delivering ansupplement.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

These and other features and advantages of the present invention willbecome more readily appreciated as the same becomes better understood byreference to the following detailed description when considered inconnection with the accompanying drawings, wherein;

FIG. 1A-1E is a fragmentary perspective view of the present invention.

FIG. 1F is a fragmentary perspective view of the suction vents inconjunction with the present invention.

FIG. 1G-1M is a perspective view showing structuring of the presentinvention.

DETAILED DESCRIPTION OF THE INVENTION

Referring to FIGS. 1A-1D, wherein like numerals indicated like orcorresponding features throughout the view, a exemplary pressurizedinjectable mouthpiece is generally shown at (1) for purpose ofillustration and not to be in any way limiting.

Specifically, referring to FIG. 1A-1D an pressurized injectablemouthpiece (1) is contoured as an U-shape object, and further made of anrubber type of material as the likes of ethyl vinyl acetate (EVA),Kraton styrene polymer material, PVC, and ENGAGE, a polyethylene polymerproduct produced by DOW chemical, or an similar material known to oneskilled in the art(s). Further, the pressurized injectable mouthpiece(1) is formed by an molding process or (SLS) 3D printing process. The 3Dprinting process may be performed by companies like Palmiga Innovationswebsite Palmiga.com, Rubber 3Dprinting website rubber3dprinting.com,i.materialise at Technologielaan 15, 3001 Leuven websitei.materialise.com, 3D-Alchemy 28 Shrewsbury Rd Edgmond Shropshire TF108HU, UK Email: info@3d-alchemy.com.uk Tel: +44 (0) 1952 820 453 CompanyNo: 301 3456 VAT No: 656138328, Amsterdam Frederiksplein 42 1017XNAmsterdam 1-347-708-1683 website 3dhubs.com.

The 3D print process may be referred to as Selective laser sintering(SLS) an additive manufacturing (AM) technique that uses an laser as thepower source to sinter powdered material (typically nylon/polyamide),aiming the laser automatically at points in space defined by an 3Dmodel, binding the material together to create a solid structure. It issimilar to direct metal laser sintering (DMLS); the two areinstantiations of the same concept but may differ in technical details.Selective laser melting (SLM) uses a comparable concept, but in SLM thematerial is fully melted rather than sintered, allowing differentproperties (crystal structure, porosity, etc.).

However, SLS involves the use of a high power laser (for example, acarbon dioxide laser) to fuse small particles of plastic, metal,ceramic, glass, or rubber powders into a mass that has a desiredthree-dimensional shape. The laser selectively fuses powdered materialby scanning cross-sections generated from a 3-D digital description ofthe part (for example from a CAD file or scan data) on the surface of apowder bed. After each cross-section is scanned, the powder bed islowered by one layer thickness, a new layer of material is applied ontop, and the process is repeated until the part is completed. Becausefinished part density depends on peak laser power, rather than laserduration, a SLS machine typically uses a pulsed laser. The SLS machinepreheats the bulk powder material in the powder bed somewhat below itsmelting point, to make it easier for the laser to raise the temperatureof the selected regions the rest of the way to the melting point.

In contrast with some other additive manufacturing processes, such asstereolithography (SLA) and fused deposition modeling (FDM), which mostoften require special support structures to fabricate overhangingdesigns, SLS does not need a separate feeder for support materialbecause the part being constructed is surrounded by unsintered powder atall times, this allows for the construction of previously impossiblegeometries. Also, since the machine's chamber is always filled withpowder material the fabrication of multiple parts has a far lower impacton the overall difficulty and price of the design because through atechnique known as “Nesting” multiple parts can be positioned to fitwithin the boundaries of the machine.

Some SLS machines use single-component powder, such as direct metallaser sintering. Powders are commonly produced by ball milling. However,most SLS machines use two-component powders, typically either coatedpowder or a powder mixture. In single-component powders, the laser meltsonly the outer surface of the particles (surface melting), fusing thesolid non-melted cores to each other and to the previous layer. Comparedwith other methods of additive manufacturing, SLS can produce parts froma relatively wide range of commercially available powder materials.These include polymers such as nylon (neat, glass-filled, or with otherfillers) or polystyrene, metals including steel, titanium, alloymixtures, and composites and green sand. The physical process can befull melting, partial melting, or liquid-phase sintering. Depending onthe material, up to 100% density can be achieved with materialproperties comparable to those from conventional manufacturing methods.In many cases large numbers of parts can be packed within the powderbed, allowing very high productivity.

SLS technology is in wide use around the world due to its ability toeasily make very complex geometries directly from digital CAD data.While it began as a way to build prototype parts early in the designcycle, it is increasingly being used in limited-run manufacturing toproduce end-use parts. One less expected and rapidly growing applicationof SLS is its use in art.

Because SLS can produce parts made from a wide variety of materials(plastics, rubber, glass, ceramics, or metals), it is quickly becoming apopular process for creating prototypes, and even final products. SLShas been increasingly utilized in industry in situations where smallquantities of high quality parts are needed, such as in the aerospaceindustry, where SLS is being used more often to create prototypes foraircraft. Aircraft are often built in small quantities and stay inservice for decades, so producing physical molds for parts becomes noncost effective, so SLS has become an excellent solution. Hence, the 3Dprinting process used in conjunction with the present invention is notlimited to any another 3D printing process such as FDM, SLA/DLP,Material Jetting, DMLS/SLM, Binder Jetting or any other 3D printingprocess known to one skilled in the art(s).

More of, the pressurized injectable mouthpiece (1) comprises an bottomportion (20) and top portion (21), further the bottom portion (20) andtop portion (21) composes an plurality of respectively spaced innerwalls (30) and outer walls (25) that curve inwardly and slightlyrecessed forming the U-shape pressurized chamber (13), which allocatesan thick density supplement as an gel-texture to arrange within thepressurized chamber (13) further allocating the supplement to deviatethe suction vents (3) when an combined pressure is applied equally tothe pressure chamber (13) outer top base (6) and outer bottom base (12).Further, the U-shaped pressurized chamber (13) is configured to retainan supplement in conjunction with pressure when the tab (2) isintroduced into the injection hole (4).

More of, the pressurized injectable mouthpiece (1) composes an injectionhole (4) approximately 3 mm to 6 mm in diameter of an quadrilateral,spherical, or elliptical shape. The injection hole (4) further comprisesan partial recessed groove region boarding the injection hole (4) edgesso that when the tab (2) is affixed at the injection hole (4) the tab(2) outer edges respectively corresponds and seats within the groovedregion thereon. The injection hole (4) comprises two respectivelyvertical walls (39) adjacently each other at the grooved region edgesthat respectively bifurcate the midpoint channel (36), left channel (37)and right channel (38) and further corresponds with the extended region(18) midpoint channel (36) left channel (37) and right channel (38).Further, the midpoint channel (36) respectively dispenses an supplementto both left and right regions of the pressurized chamber (13) via theextended region (18) midpoint channel (36), while the left channel (37)respectively dispenses an supplement to the left region of thepressurized chamber (13) via the extended region (18) left channel (37),and the opposing right channel (38) respectively dispenses an supplementat the right region of the pressurized chamber (13) via the extendedregion (18) right channel (38) whereas the combination of channels givean user an plurality of predetermine regulated options at which regionof the pressurized chamber (13) an supplement is to be dispensed.

Further, the injection hole (4) is formed at an mid center region of thepressurized injectable mouthpiece (1) front base region, furtherallowing an quadrilateral, spherical or elliptical shape package funnel,nipple or rim to introduce within the injectable hole (4) and supply angel-texture supplement within the pressurized chamber (13).

Alternatively, the injection hole (4) is formed at the mid center regionof the lip guard (9) front face, further corresponding with the hollowU-shape extended region (18). Specifically, the injection hole (4) formsan narrow hollow channel (40) within the lip guard (9) that respectivelycorresponds with the extended region (18) allocating an supplement todispense within the pressurized chamber (13) via the midpoint channel(36) left channel (37), right channel (38) or an combination thereof.

In conjunction with the injection hole (4) the tab (2) is configured toplug and restrict supplements and air from escaping the injection hole(4) region and allocating the pressurized injectable mouthpiece (1) toretain an perpetual amount of pressure in conjunction with the suctionvents (3) introducing and releasing air flow and the air pockets (5)introducing and releasing air flow when the pressurized chamber (13) iseither at an compressed or decompressed state FIG. 1B.

The pressurized injectable mouthpiece (1) comprises an quadrilateral,spherical, or elliptical-shaped tab (2) comprising an nipple (24) andflange hang (15) whereas the tab (2) is affixed to front base (44) ofpressurized injectable mouthpiece (1) and front face (45) of the lipguard (9). Optionally, the tab (2) composes an narrow quadrilateralshape flange hang (15) affixed at an rear exterior region of the tab (2)that partially extends away from the body of the tab (2). Specifically,the flange hang (15) respectively arranges approximately 6.35 mmadjacent the injection hole (4) at the left hand-side.

Additionally, the tab (2) comprises an hollow enclosed nipple (24)slightly larger than the injection hole (4) overall circumferenceaffixed centering the front face of the tab (2) forming anquadrilateral, spherical, or elliptical shape partially extending awayfrom the tab (2) body configured to respectively plug the injection hole(4) region, otherwise the tab (2) comprises an block shape nipple (24)whereas the mid-region of the block is profoundly recessed correspondingwith the injection hole (4) walls (39).

The tab (2), nipple (24), and flange hang (15) is further made of anrubber type material. Optionally, the pressurized injectable mouthpiece(1) composes an elliptical shape or quadrilateral shape with curvedcorners lip guard (9) arranged at the front base of the pressurizedinjectable mouthpiece (1), that traditionally protects the wear lipsfrom further damage. The lip guard (9) forms spaced walls configuralforming an empty hollow region allocating an thick density gelsupplement to arrange and deviate the lip guard (9) portion migrating tothe pressurized chamber (13). The lip guard (9) is approximately 44.45mm to 76.2 mm in length and 44.45 mm to 69.85 in height according tooverall dimensions. More of; optionally the lip guard (9) arranges anpair of inhalation vents (35) arranged upwardly adjacent the injectionhole (4) at opposing regions, specifically the inhalation vents (35) arerespectively incised through the front face of the lip guard (9) formingthe inhalation vents (35) imprint at the hind side of the lip guard (9).The inhalation vents (35) forms an elliptical, quadrilateral orspherical shape comprising an waffled pattern.

More of, the front base (44) of the pressurized injectable mouthpiece(1) composes an U-shaped extended region (18) that receives an midhind-side region of the lip guard (9) composing an supplement channel(60) that respectively corresponds with the injection hole (4) channel(40) that allocates an supplement to enter the extended region (18) viathe midpoint channel (36), left channel (37), right channel (38) or ancombination thereof.

The extended region (18) further arranges respective spaced top andbottom walls forming an spaced hollow region, the hollow region arrangestwo vertical walls (39) at opposing regions that respectively bifurcatethe midpoint channel (36), left channel (37) and right channel (38) ofthe supplement channel (60), additionally the supplement channel (60)corresponds with the injection hole (4) channel (40) midpoint channel(36), left channel (37) and right channel (38). Specifically, theextended region (18) outer walls (41) partially flanges outwardly fromthe front base (44) curving inwardly in direction forming an U-shapereceiving an mid hind-side region of the lip guard (9), additionally theextended region (18) inner wall (42) respectively partially flangesoutwardly from the front base (44) curving inwardly in direction backtowards the front base (44) forming an respective U-shape, whereas inconjunction the outer wall (41) and inner wall (42) forms an U-shapecomprising an partial opening (43) in-between the front base (44) andinner wall (42) FIG. 1C.

Further, the pressurized injectable mouthpiece (1) optionally comprisean quadrilateral shape tether member (10) marginally adjacent theinjection hole (4) that respectively extends from the front base (44) ofthe pressurized injectable mouthpiece (1) and font face (45) of the lipguard (9) comprising an plurality of recessed openings (23), an far endregion slightly reedier in width than the opposing body of the tethermember (10), and an fixing knot (11) arranged at the reedier edge regionthat secures the pressurized injectable mouthpiece (1) to an facemask orsimilar object FIG. 1D.

The tether member (10) is made of an rubber type material. Additionally,the tether member (10) comprises an plurality of respectively recessedopenings (23) contoured as an elliptical, spherical, or quadrilateralshape respectively correspond with the fixing knot (11) shape, arrangedthroughout its portions approximately 6.35 mm to 19.05 mm adjacent eachother. Furthermore, one end region of the tether member (10) comprisesan respective fixing knot (11) that respectively corresponds with thetether member (10) recessed openings (23) shape and is slightly largerthan the recessed openings (23) according to dimensions arranged at theedge of tether member (10) intended to introduce into at lease onerecessed opening (23) respectively securing the pressurized injectablemouthpiece (1) to an facemask. The fixing knot (11) is contoured as anelliptical, spherical, or quadrilateral shape, and is made of an rubbertype of material. More specifically, the tether member (10) isrespectively arranged approximately 6.35 mm above, below, or to theright slightly adjacent the injection hole (4).

More of, the pressurized injectable mouthpiece (1) comprises severalsuction vents (3) throughout the top outer base (6), the suction vents(3) are arranged at an horizontal pattern on the top outer base left andright side. The suction vents (3) are coutured as an crescent-moon shapefurther comprising an waffled pattern, whereas the waffled patternarranges miniature holes throughout the circumference of its patternintended to allocate an slight release of supplements from the suctionvent(s) (3) when the pressurized chamber (13) is at an compressed stateand further restricting an profoundly output of supplements when thepressurized chamber (13) is at an decompressed state. Alternatively, thesuction vents (3) are contoured as an company logo such as an NIKEswoosh logo, Jordan Jump Man logo, Puma logo, Rebook logo, Adidas logo,Under-Armor logo, are the like(s) FIG. 1E.

Further, in conjunction with the suction vents (3) and injection hole(4) they can be formed by Diamond-Drag (Scratch) Engraving using anon-rotating tool with a cone-shaped diamond tip, which is dragged withpressure through rubber material, leaving an impression. Burnishingusing a rotating tool with limited pressure, either carbide or a diamondcutter of varying tip width, to remove the top coating or layer ofrubber material resulting in a smooth, polished finish. Rotary Engravingusing a single or multiple fluted cutting tools which rotates throughthe work to remove material, leaving a trough of exposed core. Diecutting the process begins when the desired gasket shape is made into ametal die, which is essentially a strip of metal bent into the gasketshape. This metal die is pressed through a material, stamping out theshape. Laser cutting further the gasket shape is inputted into acomputer that is connected to the laser cutting machine. Then, as perthe computer's queue, a high-powered laser beam maneuvers over thematerial, cutting extremely precise lines. Hydro-jet cutting thisprocess begins similar to laser cutting since a design is first inputtedinto a computer. The computer then controls the hydro-jet cutter andsprays a high-pressured jet stream of water through the material.

Onto FIG. 1F, here shown the top inner base (7) and bottom inner base(8), further several air pockets (5) are affixed (3D printed) to theleft and right side of the top inner base (7) and bottom inner base (8).Generally, many consideration can be taken when forming and affixing theair pockets (5) at the top inner base (7) and bottom inner base (8).

Further, the air pockets (5) allocates the pressurized injectablemouthpiece (1) to be regulated by the amount of pressure respectivelyapplied to top outer base (6) and bottom outer base (12) in response toan user biting down on the pressurized injectable mouthpiece (1).Specifically, the air pockets (5) forms an hollow quadrilateral orspherical shape further comprising an plurality of mini openings (24)throughout its exterior circumference allocating air to seep in and out,in response to an user respectively biting down on the top outer base(6) and bottom outer base. Generally when an user bite down on the topouter base (6) and bottom outer base (12) pressure is applied to thepressurized chamber (13) in conjunction the air pockets (5) is at ancompressed state, further an profoundly amount of air flow is introduceat the pressurized chamber (13) through the suction vents (4) inparallel an profoundly amount of air flow is output from the miniopening (24) at the air pockets (5), upon releasing pressure from thetop outer base (6) and bottom outer base (12) in conjunction with thepressurized chamber (13) air entrapped within the pressurized chamber(13) is deviated at the suction vents (4) along with air flow entrappedwithin the air pockets (5) executing an regulated pressurized task.

In addition, the air pockets (5) are symmetrically directly coupled toeither the top inner base (7) or bottom inner base (8) leaving anpartial spacing barrier in between either the top inner base (7) orbottom inner base (8), or directly affixed to the top inner base (7) andbottom inner base (8) together with no spacing in between the top andbottom inner base (7, 8).

The air pockets (5) arranges an spacing barrier between the top innerbase (7) and bottom inner base (8) of the pressurized chamber (13)allocating an gel-type supplement of an high or low density to arrangewithin the pressurized chamber (13) without gel-blockage. Further, theair pockets (5) are made of an rubber type material.

Signifying, FIG. 1G-1M shows an structuring of the present invention.For instance, during the 3D printing process the U-shape bottom baselayer (28) is respectively formed first, in conjunction the bottom innerbase (8) of the bottom base layer (28) comprises an partial recessedregion. The bottom base layer (28) comprises an plurality of air pockets(5) respectively formed and respectively spaced approximately 3.35 mm to6.35 mm adjacent each other where at lease 4 air pockets (5) are affixedat the left and right side of the bottom inner base (8) circumference,the perpendicular length of the air pockets (5) can vary depending ifthe air pockets (5) are directly or indirectly affixed at the top innerbase (6) or bottom inner base (8).

Further, the bottom base layer (28) composes vertical outer walls (26)and inner walls (27) respectively formed following the forming of theair pockets (5), the inner walls (27) and outer walls (26) respectivelyforms an U-shape, further the front region of the outer walls (26) formsthe partial bottom portion of the U-shape extended region (18) andchannel walls (39), in conjunction an partial bottom portion lip guard(31) is formed shaped as an half-moon amid the partial spacing at thefront region in between the outer walls (26), further an partial bottomportion of the injection hole (4) and channel walls (39) is formed alongan mid region at the front face of the partial bottom portion lip guard(31). In parallel, the partial bottom portion lip guard (31) cancomprises an recessed slit (33) approximately 6.35 mm in horizontallength so that the tab (2) flange hang (15) edge region can arrangewithin. Further, the partial bottom portion lip guard (31) can comprisesan second recessed slit (34) approximately 6.35 mm to 12.07 mm inhorizontal length so that the tether member (2) edge region can arrangewithin depending on the tether member (10) arrangement adjacent theinjection hole (4) FIG. 1H.

Alternatively, when forming the air pocket (5) the laser respectivelyprints an respective reedy U-shaped intermediate layer (16) thatrespectively corresponds with the interior of the bottom base layer(28), further the intermediate layer (16) comprises an plurality of airpockets (5) respectively formed and respectively spaced approximately3.35 mm to 6.35 mm adjacent each other where at lease 4 air pockets (5)are affixed at the left and right side of the intermediate layer (16)circumference. The intermediate layer (16) is respectively affixedwithin the U-shaped bottom base layer (28) interior where the laserrespectively print tacks at edge regions of the intermediate layer (16)and bottom base layer (28) interior walls respectively affixing theintermediate layer (16) at the interior of the bottom base layer (28)FIG. 1I.

In addition, when forming the tab (2) the laser respectively prints anquadrilateral, spherical or elliptical shape tab (2) and nipple (14) atthe front face of the tab (2), further the flange hang (15) is formed atthe rear of the tab (2) partially extending outwardly in direction awayfrom the tab (2). The edge region of the flange hang (15) is furtherrespectively inserted at the lip guard (9) recessed slit, in responsethe laser respectively prints at the recessed slit region sealing theflange hang (15) within the recessed slit FIG. 1J.

Additionally, when forming the tether member (10) the laser respectivelyprints an narrow quadrilateral shape tether member (10) and anquadrilateral, spherical or elliptical shape fixing knot (11) at theedge region of the tether member (10). The edge region of the tethermember (10) is further respectively inserted at the partial bottomportion lip guard (31) recessed slit (34), in response the laserrespectively prints at the recessed slit region sealing the flange hang(15) within the recessed slit FIG. 1K.

Moreover, forming of top base layer (29) the laser starts at an topregion of the partial bottom portion of the injection hole (4) amid thefront face of the partial bottom portion lip guard (9), where an partialtop portion lip guard (32) is formed in conjunction with the partial topportion injection hole (4) and channel walls (39) forming the completestructure of the injection hole (4) and lip guard (9), further the laserprints the partial top portion U-shape extended region (18) and channelwalls (39) where walls partially extend from the hind side of the lipguard (9) back towards the front region of the outer walls (26) formingthe complete structure of the hollow U-shape extended region (18).

Furthermore, the top portion of the pressurized chamber (13) is formedwhere the laser starts at an front region of the outer walls (26),further walls partially extend inwardly and slightly curve downward atthe inner side of the outer walls (26) further curving upwardly affixingto the inner walls (27) forming the pressurized chamber (13) and furthercompleting the structure of the pressurized injectable mouthpiece (1).In parallel, the partial top portion lip guard (32) can comprises anrecessed slit (33) approximately 6.35 mm in horizontal length so thatthe tab (2) flange hang (15) edge can arrange within FIG. 1L. Thepartial top portion lip guard (32) can comprises an second recessed slit(34) approximately 6.35 mm to 12.07 mm in horizontal length so that thetether member (10) edge region can arrange within depending on thetether member (10) arrangement adjacent the injection hole (4) FIG. 1M.Examples of the above mentioned process can be better understood in U.S.Pat. Nos. 4,938,816; 5,817,206; U.S. application Ser. No. 15,118,989;U.S. Pat. No. 4,300,474; and Int Appl. Nos: PCT/EP20 17/07335 1. Oneskilled in the art(s) could understand the processes and laserpositioning.

Although the preceding description contains significant detail, itshould not be construed as limiting the scope of the invention butrather as providing illustrations of the preferred embodiment of theinvention. It is to be understood that the above description is intendedto be illustrative, and not restrictive. Many other embodiments will beapparent to those of skill in the art upon reading and understanding theabove description. The scope of the invention should, therefore bedetermined with reference to the appended claims, along with the fullscope of equivalents to which such claims are entitled.

Having described my invention, I claim:
 1. An pressurized injectablemouthpiece for athletes used in contact sports adapted for theadministration of an gel-supplement and adapted to be used at anpressurized fashion comprising: an injection hole approximately 3 mm to6 mm in diameter of an quadrilateral, spherical, or elliptical shape; aninjection hole comprising two respectively vertical walls adjacentlyeach other at the grooved region edges that respectively bifurcate themidpoint channel, left channel and right channel and further correspondswith the extended region midpoint channel left channel and rightchannel; an quadrilateral, spherical, or elliptical-shaped tabcomprising an nipple and flange hang whereas the tab is affixed to frontbase of pressurized injectable mouthpiece and front face of the lipguard; an elliptical shape or quadrilateral shape with curved cornerslip guard arranged at the front base of the pressurized injectablemouthpiece; an lip guard arranging an pair of inhalation vents arrangedupwardly adjacent the injection hole at opposing regions; an U-shapedextended region that receives an mid hind-side region of the lip guardcomposing an supplement channel that respectively corresponds with theinjection hole channel that allocates an supplement to enter theextended region via the midpoint channel, left channel, right channel oran combination thereof; an quadrilateral shape tether member marginallyadjacent the injection hole that respectively extends from the frontbase of the pressurized injectable mouthpiece and font face of the lipguard; and comprising an plurality of recessed openings; and an far endregion slightly reedier in width than the opposing body of the tethermember; and an fixing knot arranged at the reedier edge region thatsecures the pressurized injectable mouthpiece to an facemask or similarobject; an plurality of suction vents throughout the top outer base; andan plurality of air pockets affixed to the left and right side of thetop inner base and bottom inner base.
 2. The mouthguard of claim 1,wherein the injection hole further comprises an partial recessed grooveregion boarding the injection hole edges so that when the tab is affixedat the injection hole the tab outer edges respectively corresponds andseats within the grooved region thereon.
 3. The mouthguard of claim 1,wherein the midpoint channel respectively dispenses an supplement toboth left and right regions of the pressurized chamber via the extendedregion midpoint channel, while the left channel respectively dispensesan supplement to the left region of the pressurized chamber via theextended region left channel, and the opposing right channelrespectively dispenses an supplement at the right region of thepressurized chamber via the extended region right channel whereas thecombination of channels give an user an plurality of predetermineregulated options at which region of the pressurized chamber ansupplement is to be dispensed.
 4. The mouthguard of claim 1, wherein theflange hang respectively arranges approximately 6.35 mm adjacent theinjection hole at the left hand-side.
 5. The mouthguard of claim 1,wherein the tab comprises an hollow enclosed nipple slightly larger thanthe injection hole overall circumference affixed centering the frontface of the tab forming an quadrilateral, spherical, or elliptical shapepartially extending away from the tab body configured to respectivelyplug the injection hole region, otherwise the tab comprises an blockshape nipple whereas the mid-region of the block is profoundly recessedcorresponding with the injection hole walls.
 6. The mouthguard of claim1, wherein the lip guard is approximately 44.45 mm to 76.2 mm in lengthand 44.45 mm to 69.85 in height according to overall dimensions.
 7. Themouthguard of claim 1, wherein the inhalation vents forms an elliptical,quadrilateral or spherical shape comprising an waffled pattern.
 8. Themouthguard of claim 1, wherein the extended region further arrangesrespective spaced top and bottom walls forming an spaced hollow region,the hollow region arranges two vertical walls at opposing regions thatrespectively bifurcate the midpoint channel, left channel and rightchannel of the supplement channel, additionally the supplement channelcorresponds with the injection hole channel midpoint channel, leftchannel and right channel.
 9. The mouthguard of claim 1, wherein thetether member comprises an plurality of respectively recessed openingscontoured as an elliptical, spherical, or quadrilateral shaperespectively correspond with the fixing knot shape, arranged throughoutits portions approximately 6.35 mm to 19.05 mm adjacent each other. 10.The mouthguard of claim 1, wherein the fixing knot is contoured as anelliptical, spherical, or quadrilateral shape.
 11. The mouthguard ofclaim 1, wherein the tether member is respectively arrangedapproximately 6.35 mm above, below, or to the right slightly adjacentthe injection hole.
 12. The mouthguard of claim 1, wherein the suctionvents are couture as an crescent-moon shape further comprising anwaffled pattern, whereas the waffled pattern arranges miniature holesthroughout the circumference of its pattern intended to allocate anslight release of supplements from the suction vent(s) when thepressurized chamber is at an compressed state and further restricting anprofoundly output of supplements when the pressurized chamber is at andecompressed state.
 13. The mouthguard of claim 1, wherein the suctionvents are couture as an company logo.
 14. The mouthguard of claim 1,wherein the air pockets forms an hollow quadrilateral or spherical shapefurther comprising an plurality of mini openings throughout its exteriorcircumference allocating air to seep in and out, in response to an userrespectively biting down on the top outer base and bottom outer base.15. An selective laser sintering (SLS) structuring process for arrangingan pressurized injectable mouthpiece according to claim 1 comprising: anbottom base layer; and an intermediate layer
 16. The structuring processof claim 14, wherein the U-shape bottom base layer is respectivelyformed first.
 17. The structuring process of claim 14, wherein thebottom base layer comprises an plurality of air pockets respectivelyformed and respectively spaced approximately 3.35 mm to 6.35 mm adjacenteach other where at lease 4 air pockets are affixed at the left andright side of the bottom inner base circumference.
 18. The structuringprocess of claim 14, wherein the U-shaped intermediate layerrespectively corresponds with the interior of the bottom base layer,further the intermediate layer comprises an plurality of air pocketsrespectively formed and respectively spaced approximately 3.35 mm to6.35 mm adjacent each other where at lease 4 air pockets are affixed atthe left and right side of the intermediate layer circumference.